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Substantial contribution of transported emissions to organic aerosol in Beijing.

Kaspar R DaellenbachJing CaiSimo HakalaLubna DadaChao YanWei DuLei YaoFeixue ZhengJialiang MaFlorian UngeheuerAlexander L VogelDominik StolzenburgYufang HaoYongchun LiuFederico BianchiGaelle UzuJean-Luc JaffrezoDouglas R WorsnopNeil M DonahueMarkku Kulmala
Published in: Nature geoscience (2024)
Haze in Beijing is linked to atmospherically formed secondary organic aerosol, which has been shown to be particularly harmful to human health. However, the sources and formation pathways of these secondary aerosols remain largely unknown, hindering effective pollution mitigation. Here we have quantified the sources of organic aerosol via direct near-molecular observations in central Beijing. In winter, organic aerosol pollution arises mainly from fresh solid-fuel emissions and secondary organic aerosols originating from both solid-fuel combustion and aqueous processes, probably involving multiphase chemistry with aromatic compounds. The most severe haze is linked to secondary organic aerosols originating from solid-fuel combustion, transported from the Beijing-Tianjing-Hebei Plain and rural mountainous areas west of Beijing. In summer, the increased fraction of secondary organic aerosol is dominated by aromatic emissions from the Xi'an-Shanghai-Beijing region, while the contribution of biogenic emissions remains relatively small. Overall, we identify the main sources of secondary organic aerosol affecting Beijing, which clearly extend beyond the local emissions in Beijing. Our results suggest that targeting key organic precursor emission sectors regionally may be needed to effectively mitigate organic aerosol pollution.
Keyphrases
  • water soluble
  • particulate matter
  • air pollution
  • human health
  • risk assessment
  • heavy metals
  • drinking water
  • early onset